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儿童进行性假类风湿性关节炎(PPAC)。一种模拟类风湿性关节炎的遗传性疾病。

Progressive pseudorheumatoid arthritis of childhood (PPAC). A hereditary disorder simulating rheumatoid arthritis.

作者信息

Spranger J, Albert C, Schilling F, Bartsocas C, Stöss H

出版信息

Eur J Pediatr. 1983 Mar;140(1):34-40. doi: 10.1007/BF00661902.

Abstract

Five patients are described with a hereditary arthropathy affecting major and minor joints. The main features of this progressive connective tissue disorder are restricted joint mobility, osseous swelling of the interphalangeal and other joints, and platyspondyly. The condition is commonly misdiagnosed as "chronic juvenile polyarthritis with Scheuermann disease". It differs from the rheumatoid-factor-negative polyarticular form of rheumatoid arthritis and other rheumatoid spondylarthropathies by the absence of arthritic and other inflammatory changes, radiographically by the absence of destructive and the presence of dysplastic bone changes. The disorder does not seem to respond to the usual forms of antirheumatoid treatment. Histological studies showed a peculiar, nest-like clustering of chondrocytes in the resting and growth cartilage suggesting that pathogenetically this is a primary disorder of the articular cartilage.

摘要

本文描述了5例患有遗传性关节病的患者,该疾病累及大关节和小关节。这种进行性结缔组织疾病的主要特征是关节活动受限、指间关节和其他关节的骨质肿胀以及椎体扁平。该病常被误诊为“伴有休门氏病的慢性幼年型多关节炎”。它与类风湿因子阴性的类风湿关节炎多关节型以及其他类风湿性脊椎关节病不同,在于不存在关节炎及其他炎症变化,影像学上不存在破坏性改变且存在发育异常的骨质变化。该疾病似乎对常规的抗类风湿治疗无反应。组织学研究显示,在静止和生长软骨中软骨细胞呈现出一种特殊的巢状聚集,这表明从发病机制来看,这是一种原发性关节软骨疾病。

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